首页> 外文期刊>European spine journal: official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society >Clinical and radiological presentation of spinal epidural haemangiomas: Clinical series in a tertiary care centre during a 10-year period
【24h】

Clinical and radiological presentation of spinal epidural haemangiomas: Clinical series in a tertiary care centre during a 10-year period

机译:脊柱硬膜外血管瘤的临床和放射性介绍:10年期间高等教育中心临床系列

获取原文
获取原文并翻译 | 示例
       

摘要

Purpose: Haemangiomas are very frequent benign spinal tumours. However, pure epidural location is extremely rare. At present, only 52 cases have been reported in the literature during the last 10 years. We proposed to analyse clinical and radiological features of this rare entity treated in a tertiary care centre over the last 10 years. Methods: A study of a retrospective surgical series (2002-2012) was conducted. The clinic's electronic database was searched for "spinal" and/or "vertebral haemangiomas", which were treated by surgery and/or vertebroplasty. Clinical, radiological and histopathological data were analysed. Results: In total, the series comprised 30 spinal haemangiomas. There were 6 epidural (20 %), 17 vertebral (57 %) and 7 intradural lesions (23 %). There were four men and two women, mean age 28.3 years, with epidural lesions. One patient presented with localised back pain only, two with radiculopathy and focal neurological deficit, two with radiculopathy only and one with isolated focal neurological deficit, respectively. The onset of symptoms was progressive in four cases over weeks to months and sudden in two cases. Preoperative MRI imaging revealed features of meningioma, neurinoma or metastasis. Conclusion: Epidural haemangiomas are extremely rare spinal lesions. They may mimic more common spinal tumours clinically and radiologically. The usual treatment is gross total resection confirming the diagnosis histologically.
机译:目的:血管瘤是非常频繁的良性脊柱肿瘤。然而,纯硬膜外的位置极为罕见。目前,在过去10年中,文献中仅报告了52例。我们建议分析在过去10年中在第三次护理中心处理的这种罕见实体的临床和放射性特征。方法:进行了对回顾性外科系列(2002-2012)的研究。诊所的电子数据库被搜查为“脊柱”和/或“椎骨肺原瘤”,其被手术和/或椎体成形术治疗。分析了临床,放射学和组织病理学数据。结果:总共,该系列包括30个脊柱血管瘤。有6个硬膜外(20%),17个椎(57%)和7个内部病变(23%)。有四名男子和两名女性,平均年龄28.3岁,具有硬膜外病变。一名患者仅呈现局部背部疼痛,两种患有放射性病变和局灶性神经功能缺陷,两种患有无菌病变,分别与孤立的局灶性神经缺陷。在两种情况下,症状的发作在四个案例中进行了四种情况,两种情况下。术前MRI成像显示出脑膜瘤,神经肾癌或转移的特征。结论:硬膜外血管瘤是极稀有的脊柱病变。它们可能在临床上和放射学上模仿更常见的脊柱肿瘤。通常的治疗是总共总切除术,确认诊断组织学上。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号